تفاعل #939022

ord-4832937f74da4fad9f3613c487994982

معادلة التفاعل

CCCCCCCCCCCCCCCCOC(=O)C1CCCCC1C(=O)O
1,2-cyclohexanedicarboxylic acid monohexadecyl ester
C1CCOC1
tetrahydrofuran
CCCCCCCCCCCCCCCCOC(=O)C1CCCCC1C(=O)OCC
cyclohexane-1,2-dicarboxylic acid monoethyl ester monohexadecyl ester

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONwas treated with oxalyl choloride (5 g) overnight at room temperature
  2. 2
    أخرىAfter solvent removal in vacuuo the resultant acid chloride
  3. 3
    workup.DISSOLUTIONwas dissolved in 50 ml of absolute ethanol
  4. 4
    workup.ADDITIONsodium carbonate (2.2 g) was added
  5. 5
    ترشيحfiltered
  6. 6
    تركيزconcentrated in vacuuo
  7. 7
    workup.DISSOLUTIONThe light yellow liquid product was dissolved in hexane
  8. 8
    أخرىSolvent removal

الإجراء التجريبي

A mixture of 1,2-cyclohexanedicarboxylic acid monohexadecyl ester (white solid m.p.=54-55° C.) (8 g) (prepared from 1,2-cyclohexanedicarboxylic anhydride (1 eq), hexadecanol (1 eq), triethylamine (1 eq), in ethyl acetate at room temperature for 24 hours) in 50 ml of tetrahydrofuran was treated with oxalyl choloride (5 g) overnight at room temperature. After solvent removal in vacuuo the resultant acid chloride was dissolved in 50 ml of absolute ethanol, and sodium carbonate (2.2 g) was added. The mixture was stirred for 3 hours, filtered and concentrated in vacuuo. The light yellow liquid product was dissolved in hexane and passed through a pad of silica gel. Solvent removal gave cyclohexane-1,2-dicarboxylic acid monoethyl ester monohexadecyl ester (5.3 g) as a clear colorless liquid which forms a waxy solid when cooled to below room temperature.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07252865B2uspto-grants-2007_08